Here’s what it’s like to be a parent with multiple sclerosis

Some moments are seared onto your mind. For me, one of those was an otherwise normal day as a new mom to a beautiful four-month old little boy: the day that I got a call from my neurologist diagnosing me with multiple sclerosis.
When the call came, though I was already exhausted and stretched too thin as a new mom, I felt a wave of relief. Finally, I had an answer, after two years of knowing something about my body just didn’t feel right. When I hung up the phone, my husband and I hugged and said we’d figure it out. I had to stay the healthiest I could for this little boy who had entered my world just months earlier and broke my heart wide open.

Thank you Heather Millen for posting your story online.

This is a must-read story about what it’s like to have multiple sclerosis.

Stevens Point woman reaches out to help others with MS

STEVENS POINT (WAOW)– In recent months, Annette Huston of Stevens Points has raised $5500 to battle multiple sclerosis.

Doctors diagnosed Huston with MS in1995.

The disease causes communication problems between the brain and the rest of the body.

Symptoms may include: fatigue, numbness or walking problems.

“I feel like if I have this disease–I can make something good out of it,” Annette Huston says.

Fantastic work Annette and thank you for what you’re doing to support MS research.

Glasgow man, 30, with multiple sclerosis to take on Arctic trek for charity

Scott, who was diagnosed with relapsing remitting MS in 2015, will travel nearly 66km in temperatures of as low as minus 30 degrees Celsius.

He said: “Since being diagnosed with MS four years ago my motto has always been to ‘Challenge MS’ and I can’t think of any bigger challenge than the arctic trek.”

“I want to take advantage of this period of stable health that I am going through. Something I have learned from living with MS is that this can change at the drop of a hat.

Good luck Scott on your venture.

He is right multiple sclerosis can change on a dime as you can be walking one day and in a wheelchair the next day.

7-year-old Farmington Hills girl organizes bike-a-thon to fight MS

Amelia Nordhaus, 7, of Farmington Hills, is excited about her third annual bike-a-thon to raise money for the National Multiple Sclerosis Society.

For the first time this year, she’ll be riding without training wheels, says her mom, Tanya.
Amelia Nordhaus is an awesome young lady; she’s setting an example for adults. This is her third year of having a bike-a-thon and is a leading fundraiser for the National MS Society in Michigan.

Thank you, Amelia keep up the good work.

‘I choose to laugh’

FOR years, 27 year-old Janelle Boisson suffered from bouts of total paralysis and questioned her sanity, only to be diagnosed four years ago with multiple sclerosis (MS). No one else in her family has the disease.

“When I found out I had MS I was relieved that I was not crazy,” she told Sunday Newsday.

Like Janelle Boisson after years of testing I was also relieved to know what I was dealing with.

This is a great article to read because it highlights how difficult it is to diagnose someone with MS.